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Chapter 246-895 WAC

Last Update: 5/28/92

PHARMACY—GOOD MANUFACTURING PRACTICE FOR FINISHED PHARMACEUTICALS

WAC Sections

HTMLPDF246-895-010Definitions.
HTMLPDF246-895-020Finished pharmaceuticals—Manufacturing practice.
HTMLPDF246-895-030Personnel.
HTMLPDF246-895-040Buildings or facilities.
HTMLPDF246-895-050Equipment.
HTMLPDF246-895-060Production and control procedures.
HTMLPDF246-895-070Components.
HTMLPDF246-895-080Component and drug product containers and closures.
HTMLPDF246-895-090Reuse of teat dip containers and closures.
HTMLPDF246-895-100Laboratory controls.
HTMLPDF246-895-110Stability.
HTMLPDF246-895-120Expiration dating.
HTMLPDF246-895-130Packaging and labeling.
HTMLPDF246-895-140Master production and control records—Batch production and control records.
HTMLPDF246-895-150Distribution records.
HTMLPDF246-895-160Complaint files.
HTMLPDF246-895-170Variance and procedure.
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